Canonical Allele Identifier: CA2221867187

Gene: NOD2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50729824C= , CM000678.2:g.50729824C=	GRCh38
NC_000016.9:g.50763735C= , CM000678.1:g.50763735C=	GRCh37
NC_000016.8:g.49321236C=	NCBI36
NG_007508.1:g.37686C= , LRG_177:g.37686C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.*6C=	ENSP00000493088.1:n.*6C=
ENST00000646677.2:c.*657C=	ENSP00000496533.1:n.*657C=
ENST00000697428.1:n.2370C=
ENST00000641284.1:c.*6C=	ENSP00000493088.1:n.*6C=
ENST00000646677.1:c.*657C=	ENSP00000496533.1:n.*657C=
ENST00000647318.2:c.2892C= MANE Select	ENSP00000495993.1:p.Ser964=
ENST00000300589.6:c.2973C=	ENSP00000300589.2:p.Ser991=
NM_001293557.1:c.2892C=	NP_001280486.1:p.Ser964=
NM_022162.2:c.2973C=	NP_071445.1:p.Ser991=
XM_005256084.2:c.2892C=	XP_005256141.1:p.Ser964=
XM_006721242.2:c.2808C=	XP_006721305.1:p.Ser936=
XM_011523257.1:c.2469C=	XP_011521559.1:p.Ser823=
XM_011523258.1:c.2469C=	XP_011521560.1:p.Ser823=
XM_011523259.1:c.2307C=	XP_011521561.1:p.Ser769=
XM_005256084.4:c.2892C=	XP_005256141.1:p.Ser964=
XM_006721242.4:c.2808C=	XP_006721305.1:p.Ser936=
XM_011523259.2:c.2307C=	XP_011521561.1:p.Ser769=
XM_017023535.1:c.2400C=	XP_016879024.1:p.Ser800=
XM_017023536.1:c.2307C=	XP_016879025.1:p.Ser769=
XM_017023537.1:c.2307C=	XP_016879026.1:p.Ser769=
XM_017023538.1:c.2307C=	XP_016879027.1:p.Ser769=
NM_001293557.2:c.2892C=	NP_001280486.1:p.Ser964=
NM_001370466.1:c.2892C= MANE Select	NP_001357395.1:p.Ser964=
NM_022162.3:c.2973C=	NP_071445.1:p.Ser991=
NR_163434.1:n.3104C=